Water sorption isotherms and hysteresis of cement paste at moderately high temperature, up to 80 °C

被引:12
|
作者
Wang, Jiayi [1 ]
Yio, Marcus H. N. [2 ]
Zhou, Tingtao [3 ]
Wong, Hong S. [2 ]
Davie, Colin T. [1 ]
Masoero, Enrico [1 ,4 ]
机构
[1] Newcastle Univ, Sch Engn, Newcastle Upon Tyne NE1 7RU, England
[2] Imperial Coll London, Ctr Infrastructure Mat, Dept Civil & Environm Engn, London SW7 2AZ, England
[3] CALTECH, Dept Mech & Civil Engn, 1200 East Calif Blvd, Pasadena, CA 91125 USA
[4] Cardiff Univ, Sch Engn, Queens Bldg, Cardiff CF24 3AA, Wales
基金
英国工程与自然科学研究理事会;
关键词
Water sorption isotherm; Hysteresis; High temperature; Modeling; DFT simulations; Cavitation; Dynamic vapor sorption; RELATIVE-HUMIDITY; SELF-DESICCATION; PORE PRESSURE; S-H; CONCRETE; TRANSPORT; DENSITY; IMPACT; CONDENSATION; EQUILIBRIUM;
D O I
10.1016/j.cemconres.2022.107076
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The constitutive models of concrete often consider water desorption isotherms to be near-equilibrium and significantly affected by moderately high temperature, 40-80 degrees C, typically through microstructural changes. However literature data suggest that adsorption, not desorption, is near-equilibrium and moderate temperatures do not cause microstructural changes. This work supports the latter theory, through dynamic vapor sorption experiments on cement paste at 20-80 degrees C. Samples were pre-conditioned at 60% relative humidity and 20 degrees C, and isotherms were measured for several humidity ranges and testing rates. The results, corroborated by classical DFT simulations, indicate that adsorption is near-equilibrium and mostly unaffected by temperature, whereas desorption is out-of-equilibrium due to the ink-bottle effect at high humidity, and interlayer water at low humidity. Starting from the second cycle, desorption at higher temperatures features a shift of the cavitation pressure and overall a smaller hysteresis. A conceptual model of pore-specific temperature-dependent hysteresis is proposed to qualitatively explain the results.
引用
收藏
页数:12
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